Publications by authors named "Fortner J"

The pressing demand for critical metals necessitates the development of advanced ion separation technologies for circular resource economies. To separate transition metal ions, which exhibit near-identical chemical properties, adsorbents and membranes must be designed with ultraselective chemistries. We leverage the customizability of metal-organic frameworks (MOFs) to systematically study the role of material chemistry in sorption and selectivity of Co, Ni, and Cu.

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Article Synopsis
  • - The use of lithium-ion batteries has surged, resulting in a growing number of spent batteries that pose significant environmental hazards due to abandoned cathode materials.
  • - Research reveals that a specific microorganism enhances the breakdown of spent LiNiCoMnO (NCM622) cathodes, leading to about 59% dissolution of pristine and 78% of spent material under low-oxygen conditions.
  • - The study indicates that microbial respiration not only affects the dissolution of harmful metals like Li, Ni, Co, and Mn but also suggests a potential method for sustainable recovery of valuable materials from discarded batteries through bioleaching.
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Organic color centers (OCCs), generated by the covalent functionalization of single-walled carbon nanotubes, have been exploited for chemical sensing, bioimaging, and quantum technologies. However, monovalent OCCs can assume at least 6 different bonding configurations on the sp carbon lattice of a chiral nanotube, resulting in heterogeneous OCC photoluminescence emissions. Herein, we show that a heat-activated [2 + 2] cycloaddition reaction enables the synthesis of divalent OCCs with a reduced number of atomic bonding configurations.

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Indistinguishable single photons in the telecom-bandwidth of optical fibers are indispensable for long-distance quantum communication. Solid-state single photon emitters have achieved excellent performance in key benchmarks, however, the demonstration of indistinguishability at room-temperature remains a major challenge. Here, we report room-temperature photon indistinguishability at telecom wavelengths from individual nanotube defects in a fiber-based microcavity operated in the regime of incoherent good cavity-coupling.

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High-resolution imaging, 3D modeling, and quantitative analyses are equipping evolutionary biologists with new approaches to understanding the variation and evolution of the musculoskeletal system. However, challenges with interpreting DiceCT data and higher order use of modeled muscles have not yet been fully explored, and the error in and accuracy of some digital methods remain unclear. West Indian lizards are a model clade for exploring patterns in functional adaptation, ecomorphology, and sexual size dimorphism in vertebrates.

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Quantum defects in single-walled carbon nanotubes promote exciton localization, which enables potential applications in biodevices and quantum light sources. However, the effects of local electric fields on the emissive energy states of quantum defects and how they can be controlled are unexplored. Here, we investigate quantum defect sensitization by engineering an intrinsically disordered protein to undergo a phase change at a quantum defect site.

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Despite gold-based nanomaterials having a unique role in nanomedicine, among other fields, synthesis limitations relating to reaction scale-up and control result in prohibitively high gold nanoparticle costs. In this work, a new preparation procedure for lipid bilayer-coated gold nanoparticles in water is presented, using sodium oleate as reductant and capping agent. The seed-free synthesis not only allows for size precision (8-30 nm) but also remarkable particle concentration (10 mm Au).

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Anthropogenic organic carbon emissions reporting has been largely limited to subsets of chemically speciated volatile organic compounds. However, new aircraft-based measurements revealed total gas-phase organic carbon emissions that exceed oil sands industry-reported values by 1900% to over 6300%, the bulk of which was due to unaccounted-for intermediate-volatility and semivolatile organic compounds. Measured facility-wide emissions represented approximately 1% of extracted petroleum, resulting in total organic carbon emissions equivalent to that from all other sources across Canada combined.

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For membrane-based, water treatment technologies, fouling remains a significant challenge for pressure-driven processes. While many antifouling strategies have been proposed, there remains significant room for improved efficiency. Direct application of microbubbles (MBs) at a membrane surface offers a promising approach for managing interfacial fouling through continuous physical interaction(s).

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Nanobubble (NB) generation of reactive oxygen species (ROS), especially hydroxyl radical (OH), has been controversial. In this work, we extensively characterize NBs in solution, with a focus on ROS generation (as OH), through a number of methods including degradation of OH-specific target compounds, electron paramagnetic resonance (EPR), and a fluorescence-based indicator. Generated NBs exhibit consistent physical characteristics (size, surface potential, and concentration) when compared with previous studies.

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Wastewater treatment plants are critical for environmental pollution control. The role that they play in protecting the environment and public health is unquestionable; however, they produce massive quantities of excess sludge as a byproduct. One pragmatic approach to utilizing excess sludge is generating methane via anaerobic digestion.

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: Community pharmacies across the country have been adapting the ways their patients receive medications and prescription information during the COVID-19 pandemic. In order to reduce the risk of COVID-19 infection, the CDC encouraged patients to use pharmacy drive-throughs, curbside pickup, or home delivery services to obtain medications. This research study is one of the first studies to analyze how patients utilize and access Medication Management Services (MMS) in the community pharmacy setting during the COVID-19 pandemic.

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Per- and polyfluoroalkyl substances (PFAS) are a group of man-made chemicals that have been widely used in consumer, personal care, and household products for their stain- and water-repellent properties. PFAS exposure has been linked to various adverse health outcomes. Such exposure has commonly been evaluated in venous blood samples.

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The optical, structural, and magnetic properties of iron(II,III) sandwich complexes, Fe(Tp') (Tp' = bis(3,5-dimethylpyrazolyl)benzotriazolylborate), are described. The intensely colored Fe(Tp') (orange) and Fe(Tp') (purple) show strong MLCT bands. Geometric isomerism for M(Tp') is established crystallographically in the racemate of chiral -Fe(Tp').

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Single-wall carbon nanotubes in boron nitride (SWCNT@BN) are one-dimensional van der Waals heterostructures that exhibit intriguing physical and chemical properties. As with their carbon nanotube counterparts, these heterostructures can form from different combinations of chiralities, providing rich structures but also posing a significant synthetic challenge to controlling their structure. Enabled by advances in nanotube chirality sorting, clean removal of the surfactant used for solution processing, and a simple method to fabricate free-standing submonolayer films of chirality pure SWCNTs as templates for the BN growth, we show it is possible to directly grow BN on chirality enriched SWCNTs from solution processing to form van der Waals heterostructures.

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Chemical defects can create organic color centers in the graphitic lattice of single-walled carbon nanotubes. However, the underlying physics remains somewhat of a mystery. Here we show that two sp atomic defects can interact with each other in a way reminiscent of atoms bonding to form molecules.

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We use time-dependent density functional theory to investigate the possibility of hosting organic color centers in (6, 6) armchair single-walled carbon nanotubes, which are known to be metallic. Our calculations show that in short segments of (6, 6) nanotubes∼5nm in length there is a dipole-allowed singlet transition related to the quantum confinement of charge carriers in the smaller segments. The introduction ofsp3defects to the surface of (6, 6) nanotubes results in new dipole-allowed excited states.

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Aryl diazonium reactions are widely used to covalently modify graphitic electrodes and low-dimensional carbon materials, including the recent creation of organic color centers (OCCs) on single-wall carbon nanotube semiconductors. However, due to the experimental difficulties in resolving small functional groups over extensive carbon lattices, a basic question until now remains unanswered: what group, if any, is pairing with the aryl sp defect when breaking a C═C bond on the sp carbon lattice? Here, we show that water plays an unexpected role in completing the diazonium reaction with carbon nanotubes involving chlorosulfonic acid, acting as a nucleophilic agent that contributes -OH as the pairing group. By simply replacing water with other nucleophilic solvents, we find it is possible to create OCCs that feature an entirely new series of pairing groups, including -OCH, -OCH, -OCH, --OCH, and -NH, which allows us to systematically tailor the defect pairs and the optical properties of the resulting color centers.

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Organic color centers in single-walled carbon nanotubes have demonstrated exceptional ability to generate single photons at room temperature in the telecom range. Combining the color centers with pristine air-suspended nanotubes would be desirable for improved performance, but all current synthetic methods occur in solution which makes them incompatible. Here we demonstrate the formation of color centers in air-suspended nanotubes using a vapor-phase reaction.

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Organic color centers (OCCs) are atomic defects that can be synthetically created in single-walled carbon nanotube hosts to enable the emission of shortwave infrared single photons at room temperature. However, all known chemistries developed thus far to generate these quantum defects produce a variety of bonding configurations, posing a formidable challenge to the synthesis of identical, uniformly emitting color centers. Herein, we show that laser irradiation of the nanotube host can locally reconfigure the chemical bonding of aryl OCCs on (6,5) nanotubes to significantly reduce their spectral inhomogeneity.

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Remediation of groundwater impacted by per- and polyfluoroalkyl substances (PFAS) is challenging due to the strength of the carbon-fluorine bond and the need to achieve nanogram per liter drinking water targets. Previous studies have shown that ion exchange resins can serve as effective sorbents for the removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) in conventional water treatment systems. The objectives of this study were to evaluate the in situ delivery and PFAS sorption capacity of a polymer-stabilized ion exchange resin (S-IXR) consisting of Amberlite® IRA910 beads and Pluronic® F-127 in a quartz sand.

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Clonal multidrug resistance recently emerged in Rhodococcus equi, complicating the therapeutic management of this difficult-to-treat animal- and human-pathogenic actinomycete. The currently spreading multidrug-resistant (MDR) "2287" clone arose in equine farms upon acquisition, and coselection by mass macrolide-rifampin therapy, of the pRErm46 plasmid carrying the (46) macrolide-lincosamide-streptogramin resistance determinant, and of an mutation. Here, we screened a collection of susceptible and macrolide-resistant strains from equine clinical cases using a panel of 15 antimicrobials against rapidly growing mycobacteria (RGM) and nocardiae and other aerobic actinomycetes (NAA).

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The application of positively charged polymers is a common treatment strategy for the sorption and separation of dissolved hexavalent chromium Cr(VI). In particular, polyethylenimine (PEI) has been demonstrated as an effective polymer for Cr treatment due to abundant amine groups and cost-effectiveness. However, PEI as a photoactive polymer has not been previously explored for Cr treatment.

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